以色列新生儿网络和国家极低出生体重婴儿数据库

B. Reichman, G. Klinger, S. Zangen, Orna Levitzki, L. Lerner-Geva
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引用次数: 2

摘要

:以色列新生儿网络(INN)是以色列所有新生儿部门的自愿联盟。以色列国家极低出生体重婴儿数据库于1995年在INN的赞助下建立。该数据库的主要目标是应用高质量数据来评估极低出生体重婴儿的发病率和死亡率趋势;与国家数据相比较的单个新生儿病房绩效基准;护理和管理质量;规划国家、区域和体制结构及政策制定;纵向发展评估和合作研究项目。报告了出生体重≤1500 g的所有活产婴儿的数据,无论出生时的胎龄如何。从1995年到2019年,该数据库包括39000名极低出生体重婴儿和33000名母亲的报告,占以色列所有极低出生重量活产的99.5%以上。最小数据集包括父母人口统计详细信息、母亲妊娠史、治疗和并发症、产前护理、分娩详细信息、婴儿分娩状态、婴儿诊断、住院期间的程序和并发症以及出院时的结果。该数据库的主要活动涉及数据收集、整理和在每个参与新生儿重症监护室的独特年度报告中呈现数据,以及向部门、机构和政府卫生保健领导提交的年度国家报告。该数据库为INN的所有参与者提供了一个研究平台。来自15家不同医院和组织的60多名新生儿科医生、产科医生和流行病学家在数据库的背景下进行并发表了研究。以色列新生儿协会推动、启动并协调了两个主要的质量改进计划,包括所有INN合作者,旨在降低极早产儿的血流感染率和严重脑室出血率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Israel Neonatal Network and National Very Low Birth Weight Infant Database
: The Israel Neonatal Network (INN) is a voluntary consortium of all neonatal departments in Israel. The Israel National Very Low Birth Weight (VLBW) Infant Database was established in 1995 under the auspices of the INN. The main objectives of the database are the application of quality data for the assessment of morbidity and mortality trends of VLBW infants; benchmarking of individual neonatal unit performance in comparison to national data; quality of care and management; planning of national, regional and institutional structure and policy development; longitudinal developmental assessment and for collaborative research programs. Data are reported for all live born infants of birthweight ≤ 1,500 g, irrespective of the gestational age at birth. From 1995 through 2019, the database includes reports on 39,000 VLBW infants and 33,000 mothers encompassing over 99.5% of all VLBW live births in Israel. The minimal data set includes parental demographic details, maternal pregnancy history, treatments and complications, antenatal care, details of the delivery, infant's status at delivery, infant’s diagnoses, procedures and complications during hospitalization and outcome at discharge. The predominant activity of the database relates to data collection, collation and presentation of the data in unique annual reports for each of the participating Neonatal intensive care units (NICUs) and an annual national report presented to departmental, institutional and governmental health care leaders. The database provides a research platform for all participants in the INN. More than 60 neonatologists, obstetricians and epidemiologists from 15 different hospitals and organizations have undertaken and published studies in the context of the database. The Israel Neonatal Society has promoted, initiated and coordinated two major quality improvement programs encompassing all INN collaborators, aimed at reducing the rate of blood stream infections and the rate of severe intraventricular hemorrhage among very preterm infants.
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